Lentiviral vector packaging and producer cell lines yield titers equivalent to the industry-standard four-plasmid process.

ABSTRACT: Lentiviral vector (LVV)-mediated cell and gene therapies have the potential to cure diseases that currently require lifelong intervention. However, the requirement for plasmid transfection hinders large-scale LVV manufacture. Moreover, large-scale plasmid production, testing, and transfection contribute to operational risk and the high cost associated with this therapeutic modality. Thus, we developed LVV packaging and producer cell lines, which reduce or eliminate the need for plasmid transfection during LVV manufacture. To develop a packaging cell line, lentiviral packaging genes were stably integrated by random integration of linearized plasmid DNA. Then, to develop EGFP- and anti-CD19 chimeric antigen receptor-encoding producer cell lines, transfer plasmids were integrated by tr

SUBMITTER: Tridgett M 

PROVIDER: S-EPMC11401174 | biostudies-literature | 2024 Sep

REPOSITORIES: biostudies-literature